OSCR

Enhancer RNA-mediated transcriptional regulation of TDP-43 during early neural lineage specification.

Overview

Authors: Yeonju Jang1, Hyohi Lee1, Myunggeun Oh1, Jiin Moon1, Seung-Jin Kim2, Jaeil Han3, Jong-Lyul Park4, Seung-Kyoon Kim1
  1. Department of Convergent Bioscience and Informatics, and Graduate School of Biological Sciences, Chungnam National University, Daejeon, Republic of Korea
  2. Department of Biochemistry, College of Natural Sciences, Kangwon National University, Chuncheon, Republic of Korea
  3. Department of Microbiology and Molecular Biology, Chungnam National University, Daejeon, Republic of Korea
  4. Personalized Genomic Medicine Research Center, Korea Research Institute of Bioscience & Biotechnology, Daejeon, Republic of Korea
Journal: Animal cells and systems, volume 30, issue 1, pages 320-341
Dates: published online 26 March 2026
Type: Research article · Language: English
License: CC BY
Identifiers: DOI 10.1080/19768354.2026.2643998 · PMID 41908332 · PMCID PMC13023014 · OpenAlex W7140938552
Open access: gold, a free copy (OpenAlex)
Methods: Statistics, fMRI & imaging
Keywords: TDP-43, enhancer RNAs (eRNAs), embryonic stem cells (ESCs), neural lineage specification, epigenetics
Topic: Neurogenesis and neuroplasticity mechanisms (Developmental Neuroscience, Neuroscience), according to OpenAlex
Citations: not cited yet (Europe PMC); 78 references in the paper

Abstract

TAR DNA-binding protein 43 (TDP-43) is a DNA- and RNA-binding protein that regulates gene expression by modulating transcription and RNA processing. It plays pivotal roles in neuronal development and function, and its mislocalization and aggregation are major pathological features of several neurodegenerative diseases. However, the regulatory mechanisms that control Tdp-43 expression and activity during the transition from embryonic stem cells (ESCs) to neural progenitor cells (NPCs) remain poorly understood. Through integrative epigenomic and transcriptomic analyses, we identified multiple intergenic and intragenic enhancers within and around the Tdp-43 locus that generate enhancer RNAs (eRNAs). These eRNAs exhibit dynamic, region-specific expression changes and modulate Tdp-43 transcription in a stage- and context-dependent manner. Specifically, a subset of eRNAs was highly expressed in ESCs and downregulated upon differentiation, while others were selectively retained or induced in NPCs, paralleling changes in enhancer usage and histone modification states. Targeted knockdown of these eRNAs decreased Tdp-43 expression and was accompanied by changes in the expression of pluripotency- and lineage-associated markers, without implying direct control over full differentiation trajectories. These findings uncover a previously unrecognized aspect of Tdp-43 transcriptional regulation and highlight the significance of enhancer dynamics in the epigenetic regulation of TDP-43 expression during early lineage specification.

Reproduced under the paper's license (CC BY), from the paper cited above.

Code

The paper links to its data and to no code of its authors: see the Data section.

Tracing map

A tracing map links a paper to the code its authors published: this paper has none, so it has no map.

Data

Datasets cited

Versions

The history of this record: each version stored by the harvester or made by a correction of its authors or of the maintainers of its code, and what changed in its facts. The texts of the paper (its abstract, its availability statements) are not part of it; versions that changed only those are not listed.

Version 1, 30 September 2026: the first record

Recorded: type, language, journal, volume, issue, pages, dates, 8 authors, 5 keywords, 4 funders, 78 references.

Cite

This paper

Jang, Y., Lee, H., Oh, M., Moon, J., Kim, S.-J., Han, J., Park, J.-L., & Kim, S.-K. (2026). Enhancer RNA-mediated transcriptional regulation of TDP-43 during early neural lineage specification. Animal cells and systems, 30(1), 320-341. https://doi.org/10.1080/19768354.2026.2643998

BibTeX

@article{jang2026enhancer,
author = {Jang, Yeonju and Lee, Hyohi and Oh, Myunggeun and Moon, Jiin and Kim, Seung-Jin and Han, Jaeil and Park, Jong-Lyul and Kim, Seung-Kyoon},
title = {{Enhancer RNA-mediated transcriptional regulation of TDP-43 during early neural lineage specification}},
journal = {Animal cells and systems},
year = {2026},
month = mar,
volume = {30},
number = {1},
pages = {320--341},
publisher = {Taylor \& Francis},
issn = {1976-8354},
doi = {10.1080/19768354.2026.2643998},
url = {https://doi.org/10.1080/19768354.2026.2643998},
pmid = {41908332},
pmcid = {PMC13023014}
}

RIS

TY - JOUR
AU - Jang, Yeonju
AU - Lee, Hyohi
AU - Oh, Myunggeun
AU - Moon, Jiin
AU - Kim, Seung-Jin
AU - Han, Jaeil
AU - Park, Jong-Lyul
AU - Kim, Seung-Kyoon
TI - Enhancer RNA-mediated transcriptional regulation of TDP-43 during early neural lineage specification
T2 - Animal cells and systems
J2 - Anim Cells Syst (Seoul)
PY - 2026
DA - 2026/03/26
VL - 30
IS - 1
SP - 320
EP - 341
SN - 1976-8354
PB - Taylor & Francis
DO - 10.1080/19768354.2026.2643998
UR - https://doi.org/10.1080/19768354.2026.2643998
LA - en
ER -

CSL-JSON

{
"id": "10.1080/19768354.2026.2643998",
"type": "article-journal",
"title": "Enhancer RNA-mediated transcriptional regulation of TDP-43 during early neural lineage specification",
"container-title": "Animal cells and systems",
"author": [
{
"family": "Jang",
"given": "Yeonju"
},
{
"family": "Lee",
"given": "Hyohi"
},
{
"family": "Oh",
"given": "Myunggeun"
},
{
"family": "Moon",
"given": "Jiin"
},
{
"family": "Kim",
"given": "Seung-Jin"
},
{
"family": "Han",
"given": "Jaeil"
},
{
"family": "Park",
"given": "Jong-Lyul"
},
{
"family": "Kim",
"given": "Seung-Kyoon"
}
],
"container-title-short": "Anim Cells Syst (Seoul)",
"volume": "30",
"issue": "1",
"page": "320-341",
"DOI": "10.1080/19768354.2026.2643998",
"PMID": "41908332",
"PMCID": "PMC13023014",
"ISSN": "1976-8354",
"publisher": "Taylor & Francis",
"URL": "https://doi.org/10.1080/19768354.2026.2643998",
"language": "en",
"issued": {
"date-parts": [
[
2026,
3,
26
]
]
}
}

Similar papers

The papers with a page that share the most with this one: the tools found in their code, their categories, datasets, cited references and authors, the rarest counting most.

[1] doi:10.1186/s13024-026-00944-2
TDP-43: [GU]-ardian of the transcriptome.
Journal: Molecular neurodegeneration
In common: 17 references
[2] doi:10.1038/s43587-026-01166-3
Therapeutic targeting of the conserved region within the low-complexity domain of TDP-43 is neuroprotective and extends survival in amyotrophic lateral sclerosis mice.
Journal: Nature aging
In common: 7 references
[3] doi:10.1038/s41467-024-50680-8 [code]
Quantitative analysis of cis-regulatory elements in transcription with KAS-ATAC-seq.
Journal: Nature communications
In common: 8 references
[4] doi:10.1186/s13024-024-00735-7
Mis-localization of endogenous TDP-43 leads to ALS-like early-stage metabolic dysfunction and progressive motor deficits.
Journal: Molecular neurodegeneration
In common: 7 references
[5] doi:10.1126/sciadv.ady0256
Isoform-specific steric zippers drive aberrant assembly and mislocalization of shortened TDP-43.
Journal: Science advances
In common: 7 references
[6] doi:10.15252/embj.2022111719
Loss of TDP-43 oligomerization or RNA binding elicits distinct aggregation patterns.
Journal: The EMBO journal
In common: 7 references
[7] doi:10.1016/j.neuron.2026.01.018 [code]
DCPS modulates TDP-43-linked neurodegeneration through P-body-mediated RNA decay.
Journal: Neuron
In common: 7 references
[8] doi:10.1523/eneuro.0061-22.2022 [code]
Pathogenic Mutation of TDP-43 Impairs RNA Processing in a Cell Type-Specific Manner: Implications for the Pathogenesis of ALS/FTLD.
Journal: eNeuro
In common: 7 references
[9] doi:10.1016/j.isci.2025.112761
Critical impact of lysine 136 in TDP-43 phase separation, compartmentalization, and aggregation in living vertebrates.
Journal: iScience
In common: 6 references
[10] doi:10.1021/acschemneuro.4c00047
Transcriptome-Wide Profiling of Nascent RNA in Neurons with Enriched H3K27ac Signal Elevates eRNA Identification Efficiency.
Journal: ACS chemical neuroscience
In common: 6 references

Contribute

The authors of this paper can claim it, correct its record and validate its tracing map, and the maintainers of its code (its owner, or a public member of its organization) correct what it says of their repository; anyone signed in can ask for its removal. Every request goes to OSCR's own machine, which answers it; your account page follows them.

Sign in with ORCID to claim this paper as one of its authors, correct its record or validate its tracing map: when the paper's metadata lists your ORCID iD, you are recognized at once. Maintainers of its code: sign in with GitHub, then claim the repository on your account page.

Request its removal

To ask OSCR to remove this record, the copies of its authors' scripts or its tracing map, use the removal request page: signed in, you say who you are, what to remove and why, then review and confirm the request. Published rules decide every request (how).

Discussion, reproductions, activity

Discussion: code errors and mismatches between the code and the paper about this paper and its code, from readers and its authors, beside the paper and its tracing map.

Reproductions: reports from readers who ran the authors' code and did not get the paper's result, what they ran, with which environment, commit and data.

Activity: what happens around this paper: new versions of its record, its map's validation, discussions and reproductions. It opens with sign-in.